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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327612Generated: October 31, 2026

3-Cyclopentyloxy-4-methoxybenzaldehyde → 3-Cyclopentyloxy-4-methoxybenzyl alcohol

https://huagongshe.com/reaction/327612

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Cyclopentyloxy-4-methoxybenzaldehydeHCID 2735893—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product3-Cyclopentyloxy-4-methoxybenzyl alcoholHCID 11138706—

Reaction Steps

To a stirred solution of 10.42 g (47.3 mmol) of 3-cyclopentoxy-4-methoxybenzaldehyde in 100 mL of absolute ethanol was added 0.9 g (23.8 mmol) of sodium borohydride in one portion. The mixture was stirred for 1 hour at room temperature after which time the reaction was quenched with excess acetic acid, concentrated and azeotroped to dryness three times with 25 mL portions of toluene. The residue was dissolved in 100 mL of chloroform, washed with two, 25 mL portions of saturated sodium chloride, dried over magnesium sulfate, and concentrated to dryness. Liquid chromatography of the crude oil over 200 g of silica gel with 10% ethyl acetate in hexane provided an analytically pure oil after drying in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05274002
Source datasetuspto-grants-1993_12
ORD IDord-a9e5ea4e9f5c4ec4ad4d3df1f7062c26
Source noteuspto-grants-1993_12